Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • bowtie2: aligning multiple input files

    Hi all,

    I am new to using Bowtie2 and am having trouble aligning multiple input files. I have 24 sets of input sequence reads for each pair (24 files for mate 1 and 24 files for mate 2) which I hope to align to a reference genome.

    bowtie2 -x index -1 file1_*.fastq -2 file2_*.fastq -S output.sam


    I keep getting error messages: Warning: Output file was specified without -S. This will not work in future Bowtie 2 versions. Please use -S instead.
    Extra parameter(s) specified...
    Note that if <mates> files are specified using -1/-2, a <singles> file cannot
    also be specified. Please run bowtie separately for mates and singles.

    I think there is some issue in specifying multiple input files for each mate pair using the * to denote all the files which correspond to reads for each matepair. Is there something obvious I can change?

    Thank you!

  • #2
    Yes, the manual states that you must separate multiple files by a comma, which you're not doing. Have a look at this comment. It relates to STAR, but the principle is the same.

    Comment


    • #3
      Okay that makes sense, thanks for your help!

      Comment

      Latest Articles

      Collapse

      • seqadmin
        Essential Discoveries and Tools in Epitranscriptomics
        by seqadmin


        The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist on Modified Bases...
        Yesterday, 07:01 AM
      • seqadmin
        Current Approaches to Protein Sequencing
        by seqadmin


        Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
        04-04-2024, 04:25 PM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, 04-11-2024, 12:08 PM
      0 responses
      39 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 10:19 PM
      0 responses
      41 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 09:21 AM
      0 responses
      35 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-04-2024, 09:00 AM
      0 responses
      55 views
      0 likes
      Last Post seqadmin  
      Working...
      X